Generally, the project design can be divided into three portions:
Cloning ORs into pcDNA3.1+ respectively CRISPR/CAS9 system iSmeller system
Cloning ORs into pcDNA3.1+ respectively
In order to express olfactory receptors in HEK293, we cloned OR1A1 and OR1D2 in pcDNA3.1+, which is a constitutive-expression vector.
Name | Specific odor molecule | Forward primer | Reverse primer |
---|---|---|---|
OR1A1 | β- citronellol | cgtaagcttatgaccgagacatctcaggtggcccctgccggcggcagggaaaataac | tatggatccttacgaggagattctcttgttg |
OR1D2 | bourgeonal | cgtaagcttatgaccgagacatctcaggtggcccctgccggcggcgatggaggcaac | tatctcgagttatgtcagcctcttaaagtgtttatctaggagtcttcc |
Table 1: cloning ORs into pcDNA3.1+ respectively
CRISPR/CAS9 gRNA Design:
To achieve an intensified downstream signaling to enhance the detection sensitivity, we employed the CRISPR activation (CRISPRa) system to simultaneously increase the expression of the core components of olfactory receptor signaling via lentiviral transduction, including GNAL, RTP1 and RIC8B. At the endpoint, a cAMP-activated reporter gene (luciferase) is transfected to read out the signaling strength in response to specific and different range of odors.
Gene | Binding sequence | Position | Function |
---|---|---|---|
GNAL | GAAACAATTCTCGTGTAAAA | Sense sequence | cloning into lenti sgRNA(MS2)-puro backbone vector for CRISPRa(gRNA) |
GNAL | CGTCTCCGTTCATTGTGCTG | Antisense sequence | |
RIC8B | CAACCCGCCAGCCTCCGCCC | Sense sequence | |
RIC8B | GGGGGCGCGAGGCGTTTACC | Antisense sequence | |
RTP1 | CTGCAATCTCAGTTCAGGGC | Sense sequence | |
RTP1 | GGCAACCTGCCTGGTTGCCG | Antisense sequence |